Resultados de procura - Curtin, Julie

Human plasma-derived FVIII/VWD concentrate (Biostate): a review of experimental and clinical pharmacokinetic, efficacy and safety data por Harper, Paul, Favaloro, Emmanuel J., Curtin, Julie, Barnes, Chris, Dunkley, Scott

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The effect of an exercise intervention on aerobic fitness, strength and quality of life in children with haemophilia (ACTRN012605000224628) por Broderick, Carolyn R, Herbert, Robert D, Latimer, Jane, Curtin, Julie A, Selvadurai, Hiran C

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Estimation of transient increases in bleeding risk associated with physical activity in children with haemophilia por Broderick, Carolyn R, Herbert, Robert D, Latimer, Jane, Barnes, Chris, Curtin, Julie A, Monagle, Paul

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Updated Australian consensus statement on management of inherited bleeding disorders in pregnancy por Dunkley, Scott, Curtin, Julie A, Marren, Anthony J, Heavener, Robert P, McRae, Simon, Curnow, Jennifer L

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Long-Acting Recombinant Fusion Protein Linking Coagulation Factor IX with Albumin (rIX-FP) in Children: Results of a Phase 3 Trial por Kenet, Gili, Chambost, Hervé, Male, Christoph, Lambert, Thierry, Halimeh, Susan, Chernova, Tatiana, Mancuso, Maria Elisa, Curtin, Julie, Voigt, Christine, Li, Yanyan, Jacobs, Iris, Santagostino, Elena

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Final results of the PUPs B-LONG study: evaluating safety and efficacy of rFIXFc in previously untreated patients with hemophilia B por Nolan, Beatrice, Klukowska, Anna, Shapiro, Amy, Rauch, Antoine, Recht, Michael, Ragni, Margaret, Curtin, Julie, Gunawardena, Sriya, Mukhopadhyay, Sutirtha, Jayawardene, Deepthi, Winding, Bent, Fischer, Kathelijn, Liesner, Raina

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A Practical, One-Clinic Visit Protocol for Pharmacokinetic Profile Generation with the ADVATE myPKFiT Dosing Tool in Severe Hemophilia A Subjects por Blanchette, Victor S., Zunino, Laura, Grassmann, Viviane, Barnes, Chris, Carcao, Manuel D., Curtin, Julie, Jackson, Shannon, Khoo, Liane, Komrska, Vladimir, Lillicrap, David, Morfini, Massimo, Romanova, Gabriela, Stephens, Derek, Zapotocka, Ester, Rand, Margaret L., Blatny, Jan

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A novel cause of DKC1‐related bone marrow failure: Partial deletion of the 3′ untranslated region por Arthur, Jonathan W., Pickett, Hilda A., Barbaro, Pasquale M., Kilo, Tatjana, Vasireddy, Raja S., Beilharz, Traude H., Powell, David R., Hackett, Emma L., Bennetts, Bruce, Curtin, Julie A., Jones, Kristi, Christodoulou, John, Reddel, Roger R., Teo, Juliana, Bryan, Tracy M.

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A novel 33‐Gene targeted resequencing panel provides accurate, clinical‐grade diagnosis and improves patient management for rare inherited anaemias por Roy, Noémi B. A., Wilson, Edward A., Henderson, Shirley, Wray, Katherine, Babbs, Christian, Okoli, Steven, Atoyebi, Wale, Mixon, Avery, Cahill, Mary R., Carey, Peter, Cullis, Jonathan, Curtin, Julie, Dreau, Helene, Ferguson, David J. P., Gibson, Brenda, Hall, Georgina, Mason, Joanne, Morgan, Mary, Proven, Melanie, Qureshi, Amrana, Sanchez Garcia, Joaquin, Sirachainan, Nongnuch, Teo, Juliana, Tedgård, Ulf, Higgs, Doug, Roberts, David, Roberts, Irene, Schuh, Anna

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ALPK1 missense pathogenic variant in five families leads to ROSAH syndrome, an ocular multisystem autosomal dominant disorder por Williams, Lloyd B., Javed, Asif, Sabri, Amin, Morgan, Denise J., Huff, Chad D., Grigg, John R., Heng, Xiu Ting, Khng, Alexis J., Hollink, Iris H. I. M., Morrison, Margaux A., Owen, Leah A., Anderson, Katherine, Kinard, Krista, Greenlees, Rebecca, Novacic, Danica, Nida Sen, H., Zein, Wadih M., Rodgers, George M., Vitale, Albert T., Haider, Neena B., Hillmer, Axel M., Ng, Pauline C., Shankaracharya, Cheng, Anson, Zheng, Linda, Gillies, Mark C., van Slegtenhorst, Marjon, van Hagen, P. Martin, Missotten, Tom O. A. R., Farley, Gary L., Polo, Michael, Malatack, James, Curtin, Julie, Martin, Frank, Arbuckle, Susan, Alexander, Stephen I., Chircop, Megan, Davila, Sonia, Digre, Kathleen B., Jamieson, Robyn V., DeAngelis, Margaret M.

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